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EUDAMED last updated this device on Feb 17, 2026
081006243ORL11WQSOL-M Catheter Tip Syringe without Tip Cap is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Sol-Millennium Medical, Inc.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
00840368526787IRS004(01)00840368526787
European Medical Device Nomenclature — the EU product classification assigned to this device.
A02010203INFUSION AND IRRIGATION SYRINGES, CATHETER CONE, SINGLE-USE2 warnings recorded — scroll inside the panel to see all entries.
US-MF-000010890The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | — | Still on market |
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →081006243ORL11WQOn the marketSOL-M Catheter Tip Syringe with Luer Adapter081006243ORL11WQOn the marketSOL-M Catheter Tip Syringe without Needle081006243ORL11WQOn the marketSOL-M Eccentric Tip Syringe without Needle081006243SR319UUOn the marketSOL-M Eccentric Tip Syringe without Needle081006243SR319UUOn the marketSOL-M Eccentric Tip Syringe without Needle081006243SR319UUOn the marketCertificate health across this manufacturer's portfolio.
MDR 766495SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →No certificate specifically references this device's Basic UDI-DI.